9. Which reagent would you use to carry out the following conversion? 1. OsO4, NMO 2. H2 on Lindlar's catalyst, then KMnO4, H* BH3/THF then H2O2, NaOH, H₂O 4. H2O, H2SO4, HgSO4 ⑤. HCI/CH2Cl2 10. Which reagent would you use to carry out the following conversion? 1. 03 H2 on Lindlar's catalyst, then 03 3. Na/NH3(1) 4. BH3/THF then H2O2, NaOH, H₂O 5. mCPBA 11. Which reagent would you use to carry out the following conversion? 1. BH3/THF then H2O2, NaOH, H₂O H2O, H2SO4, HgSO4 3. H₂ on Lindlar's catalyst 4. H2 over Pd/C Na/NH3(1) H
9. Which reagent would you use to carry out the following conversion? 1. OsO4, NMO 2. H2 on Lindlar's catalyst, then KMnO4, H* BH3/THF then H2O2, NaOH, H₂O 4. H2O, H2SO4, HgSO4 ⑤. HCI/CH2Cl2 10. Which reagent would you use to carry out the following conversion? 1. 03 H2 on Lindlar's catalyst, then 03 3. Na/NH3(1) 4. BH3/THF then H2O2, NaOH, H₂O 5. mCPBA 11. Which reagent would you use to carry out the following conversion? 1. BH3/THF then H2O2, NaOH, H₂O H2O, H2SO4, HgSO4 3. H₂ on Lindlar's catalyst 4. H2 over Pd/C Na/NH3(1) H
Chemistry: The Molecular Science
5th Edition
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:John W. Moore, Conrad L. Stanitski
Chapter10: Fuels, Organic Chemicals, And Polymers
Section10.1: Petroleum
Problem 10.1E: Heptane, C7H16, can be catalytically reformed to make toluene, C6H5CH3, another seven-carbon...
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